A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17723306



Internal ID146972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39042493..39050328hg38UCSC Ensembl
chr19:39533133..39540968hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387836
hg197836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525933
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17723306
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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